ClinGen Allele Registry
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Canonical Allele Identifier:
CA375686118
Gene: ABO
HGNC
NCBI
Linked Data
dbSNP Id:
rs184446112
gnomAD v2:
9-136131556-G-C
gnomAD v4:
9-133256169-G-C
MyVariant Identifiers:
chr9:g.136131556G>C (hg19)
chr9:g.133256169G>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133256169G>C , CM000671.2:g.133256169G>C
GRCh38
NC_000009.11:g.136131556G>C , CM000671.1:g.136131556G>C
GRCh37
NC_000009.10:g.135121377G>C
NCBI36
NG_006669.1:g.21499C>G
NG_006669.2:g.24047C>G
Transcript Alleles
HGVS
Amino-acid change
ENST00000453660.4:n.591C>G
ENST00000647353.1:n.54-5017C>G
ENST00000651471.1:n.517C>G
ENST00000679909.1:c.28+18993C>G
ENSP00000506089.1:n.28+18993C>G
ENST00000453660.3:n.573C>G
ENST00000538324.2:c.559C>G
ENSP00000483018.1:p.Arg187Gly
ENST00000611156.4:c.559C>G
ENSP00000483265.1:p.Arg187Gly
NM_020469.2:c.562C>G
NP_065202.2:p.Arg188Gly
NM_020469.3:c.562C>G
NP_065202.2:p.Arg188Gly
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